These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

138 related articles for article (PubMed ID: 640656)

  • 1. De novo trisomy 4pter leads to q21.
    Herva R; von Wendt L
    Hum Genet; 1978 Mar; 41(2):225-30. PubMed ID: 640656
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Double partial trisomy of 6p23-pter and 9pter-q21.2 in a neonate resulting from 4:2 meiotic segregation of a maternal complex t(6;7;9)(p23;p15;q21.2) translocation.
    Cetin Z; Mihci E; Keser I; Karaali K; Berker S; Luleci G
    Genet Couns; 2012; 23(2):239-47. PubMed ID: 22876583
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A case of partial trisomy 2p23-pter syndrome with trisomy 18p due to a de novo supernumerary marker chromosome.
    Lee JH; Cho HS; Lee ES; Jung BC
    Korean J Lab Med; 2010 Jun; 30(3):312-7. PubMed ID: 20603594
    [TBL] [Abstract][Full Text] [Related]  

  • 4. De novo trisomy 9pter leads to q13.
    Kardon NB; Salwen HR; Krauss MA; Davis JG; Jenkins EC
    Hum Genet; 1977 Jun; 37(2):149-53. PubMed ID: 885535
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission. Karyotype: 46,XX, - 13, + t(13;13)(p11;q11)/46,XX,del(13)(p11).
    Fryns JP; Casaer P; Van den Berghe H
    Hum Genet; 1979 Jan; 46(2):237-41. PubMed ID: 422207
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Brief cytogenetic case report: a 4.5-year-old girl with deletion 4q syndrome--de novo, 46,XX, del(4) (pter leads to q31:).
    Young RS; Palmer CG; Bender HA; Weaver DD; Hodes ME
    Am J Med Genet; 1982 May; 12(1):103-7. PubMed ID: 7091193
    [No Abstract]   [Full Text] [Related]  

  • 7. Partial trisomy 13 plus partial trisomy 4q due to unusual segregation of translocation chromosomes.
    Fonatsch C; Flatz SD; Weitzel E
    Clin Genet; 1979 Feb; 15(2):176-82. PubMed ID: 761418
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Pericentric inversion and partial monosomy 4q associated with congenital anomalies.
    Serville F; Broustet A
    Hum Genet; 1977 Nov; 39(2):239-42. PubMed ID: 598833
    [TBL] [Abstract][Full Text] [Related]  

  • 9. ["De novo" partial trisomy 16p (author's transl)].
    Gabarrón Llamas J; Cabrerizo Portero D; Montserrat Bernal F; Rodríguez Costa T; Cabrerizo Merino C; Rodríguez López F
    An Esp Pediatr; 1981 Dec; 15(6):587-91. PubMed ID: 7337311
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Amelia, dextrocardia, asplenia, and congenital short bowel in deleted ring chromosome 4.
    Hou JW; Wang TR
    J Med Genet; 1996 Oct; 33(10):879-81. PubMed ID: 8933346
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Congenital anophthalmias: a case of trisomy 13].
    Kouassi FX; Koffi KV; Safede K; Cochard C; Cochener B
    J Fr Ophtalmol; 2006 Apr; 29(4):e10. PubMed ID: 16885798
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Precise mapping of a de novo duplication 18(q21-->q22) utilizing cytogenetic, biochemical, and molecular techniques.
    Wolff DJ; Schwartz MF; Cohen MM; Schwartz S
    Am J Med Genet; 1993 Jun; 46(5):520-3. PubMed ID: 8322813
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Phenotype of partial trisomy 8 (p21 leads to qter) in two unrelated patients with de novo translocation.
    Sachs ES; van Waveren G
    J Med Genet; 1981 Jun; 18(3):204-8. PubMed ID: 7241543
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prenatal detection of a de novo terminal inverted duplication 4p in a fetus with the Wolf-Hirschhorn syndrome phenotype.
    Beaujard MP; Jouannic JM; Bessières B; Borie C; Martin-Luis I; Fallet-Bianco C; Portnoï MF
    Prenat Diagn; 2005 Jun; 25(6):451-5. PubMed ID: 15966060
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Array-CGH and clinical findings in a patient with a small supernumerary r(8) mosaicism.
    Eyüpoğlu FC; Sünnetçi D; Cine N; Savli H; Okten A; Açikgöz EG; Sönmez FM
    Genet Couns; 2014; 25(3):305-13. PubMed ID: 25365853
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Abnormal chromosome 9 in a neonate program. Report of three cases.
    Nakamura Y; Sato E; Sakai K; Sakuma S; Hashimoto T; Sindou S
    Arch Pathol Lab Med; 1990 Feb; 114(2):185-7. PubMed ID: 2302035
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Inherited pericentric inversion of chromosome no. 2 with Robertsonian translocation (13q 14q) resulting in trisomy for chromosome 13q.
    Verma RS; Dosik H; Wexler IB
    J Genet Hum; 1977 Dec; 25(4):295-301. PubMed ID: 599332
    [TBL] [Abstract][Full Text] [Related]  

  • 18. "Pure" monosomy 21 pter leads to q21 in a girl born to a couple 46,XX,t(14;21)(p12;q22) and 46,XY,t(5;18)(q32;q22).
    Rivera H; Rivas F; Plascencia L; Cantú JM
    Ann Genet; 1983; 26(4):234-7. PubMed ID: 6607704
    [TBL] [Abstract][Full Text] [Related]  

  • 19. De novo direct duplication 7p (p11.2-->pter) in an Arab child with MCA/MR syndrome: trisomy 7p a delineated syndrome?
    Redha MA; Krishna Murthy DS; al-Awadi SA; al-Sulaiman IS; Sabry MA; el-Bahey SA; Farag TI
    Ann Genet; 1996; 39(1):5-9. PubMed ID: 9297445
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Partial trisomy 13q inherited from balanced translocation (5;13) (p14;q13).
    Coco R; del Rey G
    J Genet Hum; 1978 Dec; 26(4):303-10. PubMed ID: 752064
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.